2例青少年镰状细胞性贫血与自身免疫性溶血性贫血共存

IF 1.1 Q2 MEDICINE, GENERAL & INTERNAL Einstein-Sao Paulo Pub Date : 2024-11-29 eCollection Date: 2024-01-01 DOI:10.31744/einstein_journal/2024RC1105
Vinícius Reis Soares, Bruna Paccola Blanco, Carla Luana Dinardo, Marlene Pereira Garanito
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引用次数: 0

摘要

同种异体抗体或自身抗体的产生是镰状细胞病的并发症。长期或间歇性输血的镰状细胞病患者中有7.6-12%发生自身免疫;然而,自身抗体的临床意义尚不清楚。很少有研究关注儿童镰状细胞病和自身免疫性溶血性贫血。在此,我们介绍了两名青少年患者镰状细胞病和自身免疫性溶血性贫血的共存,重点是他们的病理生理、诊断、临床管理和结果。
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Coexistent sickle cell anemia and autoimmune hemolytic anemia in two adolescents.

The development of alloantibodies or autoantibodies is a complication observed in sickle cell disease. Autoimmunization occurs in 7.6-12% of chronically or intermittently transfused patients with sickle cell disease; however, the clinical implications of autoAbs are unclear. Few studies have focused on pediatric sickle cell disease and autoimmune hemolytic anemia. Herein, we present the coexistence of sickle cell disease and autoimmune hemolytic anemia in two adolescent patients, focusing on their pathophysiology, diagnosis, clinical management, and outcomes.

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来源期刊
Einstein-Sao Paulo
Einstein-Sao Paulo MEDICINE, GENERAL & INTERNAL-
CiteScore
2.00
自引率
0.00%
发文量
210
审稿时长
38 weeks
期刊最新文献
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